Canonical Allele Identifier: CA51770229
Gene: GNLY HGNC NCBI

Linked Data

dbSNP Id: rs761054186
MyVariant Identifiers: chr2:g.85920381G>T (hg19) chr2:g.85693258G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85693258G>T , CM000664.2:g.85693258G>T GRCh38
NC_000002.11:g.85920381G>T , CM000664.1:g.85920381G>T GRCh37
NC_000002.10:g.85773892G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000488945.5:n.48-2062G>T
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